A facile route to (+)- and (-)-trans-tetrahydro-5-oxo-2-pentylfuran-3-carboxylic acid, precursors of (+)- and (-)-methylenolactocin

被引：28

作者：

Drioli, S ^{[1
]}

Felluga, F ^{[1
]}

Forzato, C ^{[1
]}

Nitti, P ^{[1
]}

Pitacco, G ^{[1
]}

机构：

[1] UNIV TRIESTE,DIPARTIMENTO SCI CHIM,I-34127 TRIESTE,ITALY

来源：

CHEMICAL COMMUNICATIONS | 1996年 / 11期

关键词：

D O I：

10.1039/cc9960001289

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The enantioselective synthesis of the title gamma-lactone intermediates is easily achieved by employing Porcine pancreas lipase catalysed hydrolysis of the corresponding esters as the key step.

引用

页码：1289 / 1290

页数：2

共 12 条

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MURTA, MM
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[7] APPLICATION OF RADICAL CYCLISATION/IODINE ATOM-TRANSFER TO THE CHIRAL SYNTHESIS OF (-)-METHYLENOLACTOCIN
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[8] PARK BK, 1987, AGR BIOL CHEM TOKYO, V51, P3443
[9] THE FREE RADICAL ADDITION OF ALDEHYDES TO UNSATURATED POLYCARBOXYLIC ESTERS
PATRICK, TM
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1952, 17 (07) : 1009 - 1016
[10] CONCISE SYNTHESES OF NATURAL GAMMA-BUTYROLACTONES, (+)-TRANS-WHISKY LACTONE, (+)-TRANS-COGNAC LACTONE, (-)-METHYLENOLACTOCIN, (+)-NEPHROSTERANIC ACID, AND (+)-ROCCELLARIC ACID USING NOVEL CHIRAL BUTENOLIDE SYNTHONS
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (17) : 5628 - 5633

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